Progress in characterizing ABC multidrug transporters in zebrafish

被引:7
作者
Thomas, Joanna R.
Frye, William J. E. [1 ]
Robey, Robert W. [1 ]
Gottesman, Michael M. [1 ]
机构
[1] NCI, Lab Cell Biol, Ctr Canc Res, NIH, 37 Convent Dr,Room 2108, Bethesda, MD 20892 USA
关键词
Zebrafish; ABC transporter; P-glycoprotein; ABCG2; MRP1; Blood -brain barrier; Bioavailability; Cancer drug resistance; BLOOD-BRAIN-BARRIER; CANCER RESISTANCE PROTEIN; P-GLYCOPROTEIN; INCREASED SENSITIVITY; MULTIXENOBIOTIC RESISTANCE; DRUG TRANSPORTERS; ANTICANCER DRUGS; ADULT ZEBRAFISH; GENE LEADS; MRP1; ABCC1;
D O I
10.1016/j.drup.2023.101035
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Zebrafish have proved to be invaluable for modeling complex physiological processes shared by all vertebrate animals. Resistance of cancers and other diseases to drug treatment can occur owing to expression of the ATP -dependent multidrug transporters ABCB1, ABCG2, and ABCC1, either because of expression of these transporters by the target cells to reduce intracellular concentrations of cytotoxic drugs at barrier sites such as the blood-brain barrier (BBB) to limit penetration of drugs into privileged compartments, or by affecting the absorption, dis-tribution, and excretion of drugs administered orally, through the skin, or directly into the bloodstream. We describe the drug specificity, cellular localization, and function of zebrafish orthologs of multidrug resistance ABC transporters with the goal of developing zebrafish models to explore the physiological and pathophysio-logical functions of these transporters. Finally, we provide context demonstrating the utility of zebrafish in studying cancer drug resistance. Our ultimate goal is to improve treatment of cancer and other diseases which are affected by ABC multidrug resistance transporters.
引用
收藏
页数:9
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